Henny H. Lemmink

Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome

Toshio Mochizuki, Henny H. Lemmink, Mariko Mariyama et al. · Nature Genetics · 1994 · 510 citations

Mendelian Disorder, Genetic Disorder, Genetics +5

Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome

Martin Konrad, Martin Vollmer, Henny H. Lemmink et al. · Journal of the American Society of Nephrology · 2000 · 288 citations

Muscle strength and motor function throughout life in a cross‐sectional cohort of 180 patients with spinal muscular atrophy types 1c–4

Renske I. Wadman, Camiel A. Wijngaarde, Marloes Stam et al. · European Journal of Neurology · 2017 · 218 citations · Full text

Mutations in the type IV collagen α3 (COL4A3) gene in autosomal recessive Alport syndrome

Henny H. Lemmink, Toshlo MochlzukJ, Lambertus P. van den Heuvel et al. · Human Molecular Genetics · 1994 · 215 citations

Fibrosis, Unrelated Patients, Mendelian Disorder +12

Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.

Henny H. Lemmink, W Nillesen, Toshio Mochizuki et al. · Journal of Clinical Investigation · 1996 · 202 citations · Full text

Persistent Microscopic Hematuria, Genetics, Renal Pathology +16